Breunig K D
Institut für Mikrobiologie, Universität Düsseldorf, Federal Republic of Germany.
Curr Genet. 1989 Feb;15(2):143-8. doi: 10.1007/BF00435461.
The high copy number 2-microns DNA-like Kluyveromyces plasmid pKD1 was extremely unstable in Kluyveromyces lactis when carrying the gene for the regulatory protein LAC9, a transcriptional activator involved in the induction of the LAC and GAL genes. Transformants of a lac9 mutant strain normally contained rearranged plasmids and all were Lac-, indicating that the LAC9 gene was inactive. Lac+ "revertants" could be obtained from Lac- transformants by selection on lactose plates. In some of these, the pKD1-based plasmid was stably maintained by being integrated into the chromosome of the cell; in others, the disrupted chromosomal gene was restored by a gene conversion event. None of the Lac+ revertants had more than one intact LAC9 gene, an indication that LAC9 overexpression affects cell viability.
高拷贝数的2微米DNA样克鲁维酵母质粒pKD1在乳酸克鲁维酵母中携带调节蛋白LAC9(一种参与LAC和GAL基因诱导的转录激活因子)的基因时极其不稳定。lac9突变菌株的转化体通常含有重排的质粒,且均为Lac-,这表明LAC9基因无活性。通过在乳糖平板上筛选,可从Lac-转化体中获得Lac+“回复体”。在其中一些回复体中,基于pKD1的质粒通过整合到细胞染色体中而得以稳定维持;在另一些回复体中, disrupted染色体基因通过基因转换事件得以恢复。没有一个Lac+回复体具有超过一个完整的LAC9基因,这表明LAC9过表达会影响细胞活力。